Concepedia

Publication | Open Access

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

DOIFull Paper Access

30

Citations

48

References

2021

Year

Francesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, Abbas Tafakhori, Saghar Ghasemi Firouzabadi, Marjan Chapi, Hafiz Muhammad Azhar Baig, Alexandre Reymond, Stylianos E. Antonarakis, Muhammad Ansar
npj Genomic Medicine

References

YearCitations

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